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X chromosome-linked muscular dystrophy (mdx) in the mouse
Open accessAbstract
An X chromosome-linked mouse mutant (gene symbol, mdx) has been found that has elevated plasma levels of muscle creatine kinase and pyruvate kinase and exhibits histological lesions characteristic of muscular dystrophy. The mutants show mild clinical symptoms and are viable and fertile. Linkage analysis with four X chromosome loci indicates that mdx maps in the Hq Bpa region of the mouse X chromosome. This gives a gene order of mdx-Tfm-Pgk-1-Ags, the same as for the equivalent genes on the human X chromosome.
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“The mdx (dystrophin deficient) mouse model has a rather mild cardiomyopathy, mild limb-skeletal muscle dysfunction, and a normal life span, in contrast to human counterparts”
From Small and large animal models in cardiac contraction research: advantages and disadvantages (2014) · cites this paper as Bulfield, et al., 1984
In the citing paper
“The most widely used animal model for DMD, the mdx mouse, exhibits only a mild dystrophic phenotype, although like DMD patients, it lacks functional dystrophin due to a point mutation in the dystrophin gene (Bulfield et al., 1984; Hoffman et al., 1987; Ryder-Cook et al., 1988).”
From Short Telomeres and Stem Cell Exhaustion Model Duchenne Muscular Dystrophy in mdx/mTR Mice (2010) · cites this paper as Bulfield et al., 1984
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Gene Action in the X-chromosome of the Mouse (Mus musculus L.)
LYON, M. F. (1961) · Nature · doi:10.1038/190372a0 · Cited by 3,978
Murray, J., Davies, K. E., Harper, P. S., Meredith, L., Mueller, C. R., & Williamson, R. (1982) · Nature · doi:10.1038/300069a0 · Cited by 330
ACID HYDROLASES AS MODELS OF GENETIC CONTROL
Paigen, K. (1979) · Annual Review of Genetics · doi:10.1146/annurev.ge.13.120179.002221 · Cited by 233
Kingston, H. M., Thomas, N. S. T., Pearson, P. L., Sarfarazi, M., & Harper, P. S. (1983) · Journal of Medical Genetics · doi:10.1136/jmg.20.4.255 · Cited by 90
Chimaera mouse study shows absence of disease in genetically dystrophic muscle
Peterson, A. C. (1974) · Nature · doi:10.1038/248561a0 · Cited by 59
Serum pyruvate kinase in muscle disease and carrier states
Alberts, M. C., & Samaha, F. J. (1974) · Neurology · doi:10.1212/wnl.24.5.462 · Cited by 54
A histological study of muscle from the bar harbor strain of dystrophic mice
Pearce, G. W., & Walton, J. N. (1963) · The Journal of Pathology and Bacteriology · doi:10.1002/path.1700860105 · Cited by 51
Polymorphism of kidney pyruvate kinase in the mouse is determined by a gene, Pk-3, on chromosome 9
Peters, J., Nash, H., Eicher, E. M., & Bulfield, G. (1981) · Biochemical Genetics · doi:10.1007/bf00484007 · Cited by 46
Self-citationPyruvate kinase isoenzymes in progressive muscular dystrophy and in acute myocardial infarction
Harano, Y., Adair, R., Vignos, P. J., Miller, M., & Kowal, J. (1973) · Metabolism · doi:10.1016/0026-0495(73)90041-3 · Cited by 41
Creatine Phosphokinase Isoenzymes in Muscle in human Myopathies
Kar, N. C., & Pearson, C. M. (1965) · American Journal of Clinical Pathology · doi:10.1093/ajcp/43.3.207 · Cited by 40
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Nowend, K. L., Starr-Moss, A. N., & Murphy, K. E. (2011) · Mammalian Genome · doi:10.1007/s00335-011-9348-0 · Cited by 22
Martin, P. T., Golden, B., Okerblom, J., Camboni, M., Chandrasekharan, K., Xu, R., Varki, A. P., Flanigan, K. M., & Kornegay, J. N. (2014) · PLoS ONE · doi:10.1371/journal.pone.0088226 · Cited by 22
Mosqueira, M., Willmann, G., Ruohola‐Baker, H., & Khurana, T. S. (2010) · PLoS ONE · doi:10.1371/journal.pone.0013450 · Cited by 22
TAT-μUtrophin mitigates the pathophysiology of dystrophin and utrophin double-knockout mice
Call, J. A., Ervasti, J. M., & Lowe, D. A. (2011) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00248.2011 · Cited by 22
Chadwick, J. A., Hauck, J. S., Gómez-Sánchez, C. E., Gómez-Sánchez, E. P., & Rafael‐Fortney, J. A. (2017) · Physiological Genomics · doi:10.1152/physiolgenomics.00128.2016 · Cited by 22
Greenberg, M. J., Daily, N., Wang, A., Conway, M. K., & Wakatsuki, T. (2018) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2018.00120 · Cited by 22
A conserved annexin A6–mediated membrane repair mechanism in muscle, heart, and nerve
Demonbreun, A. R., Bogdanovic, E., Vaught, L. A., Reiser, N. L., Fallon, K. S., Long, A. M., Oosterbaan, C. C., Hadhazy, M., Page, P., Joseph, P. R. B., et al. (2022) · JCI Insight · doi:10.1172/jci.insight.158107 · Cited by 22
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Slater, C. R., & Schiaffino, S. (2008) · Springer eBooks · doi:10.1007/978-1-4020-6768-6_14 · Cited by 23
Effects of a CRF2R agonist and exercise on mdx and wildtype skeletal muscle
Hall, J. E., Kaczor, J. J., Hettinga, B. P., Isfort, R. J., & Tarnopolsky, M. A. (2007) · Muscle & Nerve · doi:10.1002/mus.20820 · Cited by 22
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Roy, F. L., Charton, K., Lorson, C. L., & Richard, I. (2009) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2009.10.005 · Cited by 22
Skynner, M. J., Drage, D., Dean, W., Turner, S., Watt, D. J., & Allen, N. D. (1999) · The International Journal of Developmental Biology · doi:10.1387/ijdb.10213086 · Cited by 22
Gene therapy in Duchenne muscular dystrophy
Inui, K., Okada, S., & Dickson, G. (1996) · Brain and Development · doi:10.1016/0387-7604(96)00043-5 · Cited by 22
Autotransplantation in mdx Mice of mdx Myoblasts Genetically Corrected by an HSV-1 Amplicon Vector
Bujold, M., Caron, N. J., Camiran, G., Mukherjee, S., Allen, P. D., Tremblay, J. P., & Wang, Y. (2002) · Cell Transplantation · doi:10.3727/000000002783985297 · Cited by 22
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Gu??rette, B., Gingras, M., Wood, K. J., Roy, R., & Tremblay, J. P. (1996) · Transplantation · doi:10.1097/00007890-199610150-00015 · Cited by 22
Ho, P. P.-K., Lahey, L. J., Mourkioti, F., Kraft, P. E., Filareto, A., Brandt, M., Magnusson, K. E. G., Finn, E. E., Chamberlain, J. S., Robinson, W. H., et al. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1808648115 · Cited by 22
Kiriaev, L., Kueh, S. L. L., Morley, J. W., Houweling, P. J., Chan, S., North, K. N., & Head, S. I. (2021) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00122.2021 · Cited by 21
Domenig, S. A., Bundschuh, N., Lenardič, A., Ghosh, A., Kim, I., Qabrati, X., D’Hulst, G., & Bar‐Nur, O. (2022) · Stem Cell Reports · doi:10.1016/j.stemcr.2021.12.003 · Cited by 21
Louboutin, J. P., Fichter-Gagnepain, V., Pastoret, C., Thaon, E., Noireaud, J., Sébille, A., & Fardeau, M. (1995) · Neuromuscular Disorders · doi:10.1016/0960-8966(95)00006-9 · Cited by 21
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Selsby, J. T., Morris, C. A., Morris, L. D., & Sweeney, H. L. (2012) · PLoS Currents · doi:10.1371/4f84a944d8930 · Cited by 21
Human artificial chromosomes for Duchenne muscular dystrophy and beyond: challenges and hopes
Tedesco, F. S. (2015) · Chromosome Research · doi:10.1007/s10577-014-9460-6 · Cited by 21
Lopez, J. R., Kolster, J., Zhang, R., & Adams, J. A. (2017) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2017.06.004 · Cited by 21
Gawlik, K. I. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19051490 · Cited by 23
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Marques, M. J., Machado, R. V., Minatel, E., & Neto, H. S. (2007) · Muscle & Nerve · doi:10.1002/mus.20892 · Cited by 21
Graciotti, L., Becker, J., Granata, A. L., Procopio, A. D., Tessarollo, L., & Fulgenzi, G. (2011) · PLoS ONE · doi:10.1371/journal.pone.0027034 · Cited by 21
López, S. M., Hammond, J. J., Rigsby, M. B., Balog-Alvarez, C. J., Kornegay, J. N., & Nghiem, P. P. (2018) · Skeletal Muscle · doi:10.1186/s13395-018-0162-1 · Cited by 21
Does muscular dystrophy affect metabolic rate?
Dupont‐Versteegden, E. E., Baldwin, R. A., McCarter, R., & Vonlanthen, M. G. (1994) · Journal of the Neurological Sciences · doi:10.1016/0022-510x(94)90353-0 · Cited by 21
Vannucchi, M. G., Zizzo, M. G., Zardo, C., Pieri, L., Serio, R., Mulè, F., & Faussone‐Pellegrini, M. S. (2003) · Journal of Cellular Physiology · doi:10.1002/jcp.10470 · Cited by 21
Lynch, G. S., Hayes, A., Lam, M. H. C., & Williams, D. A. (1993) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.1993.0078 · Cited by 21
Lack of myoblasts migration between transplanted and host muscles of mdx and normal mice
Moens, P., Schoor, M. C., & Marchal, G. (1996) · Journal of Muscle Research and Cell Motility · doi:10.1007/bf00140322 · Cited by 21
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Johnson, M. C., Payne, R. M., Grant, J. W., & Strauss, A. W. (1995) · Annals of Medicine · doi:10.3109/07853899509002580 · Cited by 21
Bittner, R. E., Popoff, I., Shorny, S., Höger, H., & Wachtler, F. J. (1997) · Anatomy and Embryology · doi:10.1007/s004290050036 · Cited by 21
Matsuda, S., Desaki, J., Fujita, H., Okumura, N., & Sakanaka, M. (1992) · Cell and Tissue Research · doi:10.1007/bf00645060 · Cited by 21
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Arcangelis, V. D., Serra, F., Cogoni, C., Vivarelli, E., Monaco, L., & Naro, F. (2010) · PLoS ONE · doi:10.1371/journal.pone.0012098 · Cited by 20
Moraes, L. H. R., de Burgos, R. R., Macedo, A. B., Hermes, T. D. A., de‐Faria, F. M., & Minatel, E. (2015) · Biological Trace Element Research · doi:10.1007/s12011-015-0290-y · Cited by 20
Marshall, J. L., Kwok, Y., McMorran, B. J., Baum, L. G., & Crosbie, R. H. (2013) · FEBS Journal · doi:10.1111/febs.12295 · Cited by 21
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Roberts, N. W., Holley-Cuthrell, J., González-Vega, M., Mull, A. J., & Heydemann, A. (2015) · BioMed Research International · doi:10.1155/2015/131436 · Cited by 20
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Gawlik, K. I., Holmberg, J., & Durbeej, M. (2014) · American Journal Of Pathology · doi:10.1016/j.ajpath.2013.11.017 · Cited by 20
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Guido, A. N., Campos, G. E. R., Neto, H. S., Marques, M. J., & Minatel, E. (2010) · The Anatomical Record · doi:10.1002/ar.21224 · Cited by 20
Gieseler, K., Grisoni, K., Mariol, M., & Ségalat, L. (2002) · Neuromuscular Disorders · doi:10.1016/s0960-8966(01)00330-3 · Cited by 20
Nico, B., Mangieri, D., Luca, A. D., Corsi, P., Benagiano, V., Tamma, R., Annese, T., Longo, V., Enrico Crivellato, B., & Ribatti, D. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.04.028 · Cited by 20
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Bagher, P., Duan, D., & Segal, S. S. (2010) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01106.2010 · Cited by 20
Fiedler, L. R., Maifoshie, E., & Schneider, M. D. (2014) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/b978-0-12-397920-9.00002-0 · Cited by 20
Kogelman, B., Putker, K., Hulsker, M., Winter, C. T.-D., van der Weerd, L., Aartsma-Rus, A. M., & van Putten, M. (2018) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2018.10.008 · Cited by 20
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Nakae, Y., Stoward, P. J., Shono, M., & MATSUZAKI, T. (1999) · Histochemistry and Cell Biology · doi:10.1007/pl00007906 · Cited by 20
Specific isomyosin proportions in hyperexcitable and physiologically denervated mouse muscle
Agbulut, O., Noirez, P., Butler-Browne, G. S., & Jockusch, H. (2004) · FEBS Letters · doi:10.1016/s0014-5793(04)00179-6 · Cited by 20
McDougall, J. J., Bray, R. C., & Sharkey, K. A. (1997) · The Anatomical Record · doi:10.1002/(sici)1097-0185(199705)248:1 · Cited by 97
Jackson, C. E., Amato, A. A., & Barohn, R. J. (1996) · Muscle & Nerve · doi:10.1002/(sici)1097-4598(199609)19:9 · Cited by 61
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Jockusch, H., Friedrich, G., & Zippel, M. (1990) · Muscle & Nerve · doi:10.1002/mus.880130613 · Cited by 20
Wang, Y. C., & Rubenstein, P. A. (1992) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)49797-4 · Cited by 20
Shibuya, S., & Wakayama, Y. (1988) · Acta Neuropathologica · doi:10.1007/bf00688102 · Cited by 20
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Boyd, Y., Blair, H. J., Cunliffe, P., Masson, W. K., & Reed, V. (2000) · Genome Research · doi:10.1101/gr.10.3.277 · Cited by 20
Gargan, S., Dowling, P., Zweyer, M., Henry, M. A., Meleady, P., Swandulla, D., & Ohlendieck, K. (2022) · Life · doi:10.3390/life12111679 · Cited by 19
Otto, A., Macharia, R., Matsakas, A., Valášek, P., Mankoo, B. S., & Patel, K. (2010) · Developmental Biology · doi:10.1016/j.ydbio.2010.04.014 · Cited by 20
Moorwood, C. (2008) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-008-8306-9 · Cited by 19
Feng, S.-W., Chen, F., Cao, J., Yu, M.-J., Liang, Y., Song, X.-M., & Zhang, C. (2012) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2012.01.029 · Cited by 19
Aigner, B., Rathkolb, B., Klaften, M., Sedlmeier, R., Klempt, M., Wagner, S., Michel, D., Mayer, U., Klopstock, T., de Angelis, M. H., et al. (2009) · Experimental Physiology · doi:10.1113/expphysiol.2008.045864 · Cited by 19
Lu‐Nguyen, N., Ferry, A., Schnell, F. J., Hanson, G. J., Popplewell, L. J., Dickson, G., & Malerba, A. (2019) · Human Molecular Genetics · doi:10.1093/hmg/ddz125 · Cited by 19
Omosule, C. L., Gremminger, V. L., AGUILLARD, A., Jeong, Y., Harrelson, E. N., Miloscio, L., Mastaitis, J. W., Rafique, A., Kleiner, S., Pfeiffer, F. M., et al. (2020) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.4223 · Cited by 21
Giacomotto, J., Ségalat, L., Carre-Pierrat, M., & Gieseler, K. (2011) · Methods · doi:10.1016/j.ymeth.2011.10.010 · Cited by 19
Amali, A. A., Lin, C. J., Chen, Y., Wang, W.-L., Gong, H., Rekha, R. D., Lu, J., Chen, T. T., & Wu, J. (2008) · Journal of Biomedical Science · doi:10.1007/s11373-008-9250-2 · Cited by 19
Expression of the glucose transporter GLUT4 in the muscular dystrophic mdx mouse
Olichon‐Berthe, C., Gautier, N., OBBERGHEN, E. V., & MARCHAND‐BRUSTEL, Y. L. (1993) · Biochemical Journal · doi:10.1042/bj2910257 · Cited by 19
Sánchez, L., Beltrán, E., Stefani, A. D., Guo, L. T., Shea, A., Shelton, G. D., Risio, L. D., & Burmeister, L. M. (2018) · PLoS ONE · doi:10.1371/journal.pone.0193372 · Cited by 19
Coles, C. A., Gordon, L., Hunt, L. C., Webster, T., Piers, A. T., Kintakas, C., Woodman, K. G., Touslon, S. L., Smythe, G. M., White, J. D., et al. (2019) · Human Molecular Genetics · doi:10.1093/hmg/ddz266 · Cited by 20
Branco, D. M., Wolf, C. M., Sherwood, M., Hammer, P. E., Kang, P. B., & Berul, C. I. (2007) · Journal of Interventional Cardiac Electrophysiology · doi:10.1007/s10840-007-9168-z · Cited by 19
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Anderson, J. E. (1991) · Biochemistry and Cell Biology · doi:10.1139/o91-124 · Cited by 19
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Worton, R. G., & Burghes, A. H. M. (1988) · International review of neurobiology · doi:10.1016/s0074-7742(08)60083-5 · Cited by 19
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Gutmann, D. H., & Fischbeck, K. H. (1989) · Annals of Neurology · doi:10.1002/ana.410260202 · Cited by 19
Lipid peroxide and antioxidant enzymes in muscle and nonmuscle of dystrophic mouse
Asayama, K., Hayashibe, H., Dobashi, K., & Kato, K. (1989) · Muscle & Nerve · doi:10.1002/mus.880120907 · Cited by 19
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Wada, E., Yoshida, M., Kojima, Y., Nonaka, I., Ohashi, K., Nagata, Y., Shiozuka, M., Date, M., Higashi, T., Nishino, I., et al. (2014) · American Journal Of Pathology · doi:10.1016/j.ajpath.2014.07.007 · Cited by 18
Porcari, P., Hall, M. G., Clark, C. A., Greally, E., Straub, V. W., & Blamire, A. M. (2020) · NMR in Biomedicine · doi:10.1002/nbm.4276 · Cited by 18
Rovina, D., Castiglioni, E., Niro, F., Mallia, S., Pompilio, G., & Gowran, A. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21196997 · Cited by 18
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Singh, R., Millman, G., Turin, E., Polisiakeiwicz, L., Lee, B., Gatti, F., Berge, J., Smith, E., Rutter, J., Sumski, C. A., et al. (2009) · Journal of the Neurological Sciences · doi:10.1016/j.jns.2009.06.030 · Cited by 18
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Miles, L., Miles, M. V., Tang, P., Horn, P. S., Quinlan, J. G., Wong, B. L. Y., Wenisch, A., & Bove, K. E. (2005) · Clinica Chimica Acta · doi:10.1016/j.cccn.2005.04.009 · Cited by 18
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Calyjur, P. C., de Almeida, C., Ayub-Guerrieri, D., Ribeiro, A. F., Fernandes, S., Ishiba, R., dos Santos, A. L. F., Onofre-Oliveira, P. C. G., & Vainzof, M. (2016) · PLoS ONE · doi:10.1371/journal.pone.0150748 · Cited by 18
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Zschüntzsch, J., Meyer, S., Shahriyari, M., Kummer, K., Schmidt, M., Kummer, S., & Tiburcy, M. (2022) · Cells · doi:10.3390/cells11071233 · Cited by 21
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Anderson, J. L., Head, S. I., & Morley, J. W. (2012) · InTech eBooks · doi:10.5772/24928 · Cited by 18
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Jüllig, M., Zhang, V. W., & Stott, N. S. (2004) · ANZ Journal of Surgery · doi:10.1046/j.1445-1433.2003.documendoc.doc.x · Cited by 18
Wuebbles, R. D., Sarathy, A., Kornegay, J. N., & Burkin, D. J. (2013) · Disease Models & Mechanisms · doi:10.1242/dmm.012211 · Cited by 19
SPASSOV, A. W., Gredes, T., Gedrange, T., Lucke, S., Morgenstern, S., Pavlović, D., & Kunert‐Keil, C. (2010) · European Journal of Orthodontics · doi:10.1093/ejo/cjq113 · Cited by 18
Tamaki, T., & Akatsuka, A. (1994) · The Anatomical Record · doi:10.1002/ar.1092400208 · Cited by 18
Nerve‐terminal and Schwann‐cell response after nerve injury in the absence of nitric oxide
Marques, M. J., Pereira, E. C. L., Minatel, E., & Neto, H. S. (2006) · Muscle & Nerve · doi:10.1002/mus.20576 · Cited by 18
Design of Trans-Splicing Adeno-Associated Viral Vectors for Duchenne Muscular Dystrophy Gene Therapy
Lai, Y., Li, D., Yue, Y., & Duan, D. (2008) · Methods in molecular biology · doi:10.1007/978-1-59745-237-3_16 · Cited by 18
Neto, H. S., Martins, A. J., Minatel, E., & Marques, M. J. (2003) · Neuroscience Letters · doi:10.1016/s0304-3940(03)00220-9 · Cited by 18
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Mokhtarian, A., Decrouy, A., Chinet, A., & Even, P. C. (1996) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/bf02191899 · Cited by 18
Dystrophin expression in the hair cells of the cochlea
Dodson, H. C., Piper, T. A., Clarke, J. D. W., Quinlivan, R. C. M., & Dickson, G. (1995) · Journal of Neurocytology · doi:10.1007/bf01257377 · Cited by 18
Quantification of normal dystrophin mRNA following myoblast transplantation in mdx mice
Asselin, I., Tremblay, M. W., Vilquin, J., Guérette, B., Roy, R., & Tremblay, J. P. (1995) · Muscle & Nerve · doi:10.1002/mus.880180909 · Cited by 18
Quinlan, J. G., Johnson, S. R., & Samaha, F. J. (1990) · Muscle & Nerve · doi:10.1002/mus.880130316 · Cited by 18
DWORF Gene Therapy Improves Cardiac Calcium Handling and Mitochondrial Function
Brito‐Estrada, O., Kuwabara, Y., Gibson, A. M., Hassel, K. R., Kamradt, M. L., Verry, J. P., Blair, N. S., Bround, M. J., Huo, J., Molkentin, J. D., et al. (2025) · Circulation Research · doi:10.1161/circresaha.125.326550 · Cited by 17
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Burns, D. P., & O’Halloran, K. D. (2015) · Respiratory Physiology & Neurobiology · doi:10.1016/j.resp.2015.12.001 · Cited by 17
Basser (2000) · doi:10.1002/1522-2594(200010)44:4
Metadata
- Authors
- Bulfield, G., Siller, W. G., Wight, P. A., & Moore, K. J.
- ORCID
- Wight, P A
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 1984-02
- Volume
- 81
- Issue
- 4
- Pages
- 1189-1192
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC344791
- OpenAlex
- W2070936696
- Cited by
- 1,765
- References
- 17
- Citations by year
- 2026: 24 · 2025: 46 · 2024: 47 · 2023: 56 · 2022: 54 · 2021: 60 · 2020: 65 · 2019: 38 · 2018: 68 · 2017: 60 · 2016: 54 · 2015: 78 · 2014: 79 · 2013: 58 · 2012: 65
- FWCI
- 3.64
- Type
- journal article
- Language
- en
- Open access
- green
- europepmc.org
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- The Mouseion at the JAXlibrary (Jackson Laboratory) (submittedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
- Health Sciences › Medicine › Genetics (clinical) › Neurogenetic and Muscular Disorders Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genomics and Rare Diseases
- Keywords
- X-linked muscular dystrophy, Duchenne muscular dystrophy, muscle creatine kinase, pyruvate kinase, X chromosome mapping, gene order
- MeSH terms
- Animals, Crosses, Genetic, Female, Genetic Linkage, Male, Mice, Inbred C57BL, Mice, Mutant Strains, Muscles, Muscular Dystrophy, Animal, Mutation, Pyruvate Kinase, X Chromosome, Mice
About these checks
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